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FDA 510(k)

FORCEPS FOR LAPAROSCOPIC SURGERY GU USE

K-Number: K925959 · 1993-11-12

ApplicantZinnanti Surgical Instruments, Inc.
Decision Date1993-11-12
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FORCEPS FOR LAPAROSCOPIC SURGERY GU USE is the device name listed in this FDA 510(k) record. The listed applicant is Zinnanti Surgical Instruments, Inc.. It received FDA 510(k) clearance on 1993-11-12 under 510(k) number K925959. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FORCEPS FOR LAPAROSCOPIC SURGERY GU USE?

FORCEPS FOR LAPAROSCOPIC SURGERY GU USE is a medical device that received FDA 510(k) clearance on 1993-11-12. The listed applicant is Zinnanti Surgical Instruments, Inc.. The 510(k) number is K925959.

When did FORCEPS FOR LAPAROSCOPIC SURGERY GU USE receive FDA 510(k) clearance?

FORCEPS FOR LAPAROSCOPIC SURGERY GU USE received FDA 510(k) clearance on 1993-11-12, under 510(k) number K925959.

Who is the listed applicant for FORCEPS FOR LAPAROSCOPIC SURGERY GU USE?

The FDA 510(k) record lists Zinnanti Surgical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORCEPS FOR LAPAROSCOPIC SURGERY GU USE?

The FDA product code for FORCEPS FOR LAPAROSCOPIC SURGERY GU USE is GCJ.

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Other records listing Zinnanti Surgical Instruments, Inc. as applicant

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Related Devices (Code: GCJ)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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